Bathophenanthroline

Bathophenanthroline Basic information
Classification Applications Reactions
Product Name:Bathophenanthroline
Synonyms:BATHOPHENANTHROLINE;TIMTEC-BB SBB008862;4,7-Diphenyl-1,1-phenanthroline;4,7-DIPHENYL-1,10-PHENANTHROLINE;1,10-bathophenanthroline;bathophenanthrolin;4,7-DIPHENYL-1,10-PHENANTHRO-;BATHOPHENANTHROLINE R. G.
CAS:1662-01-7
MF:C24H16N2
MW:332.4
EINECS:216-767-1
Product Categories:organic amine;oled materials;Analytical Chemistry;Chelating Reagents;Achiral Nitrogen;Py-N;Electroluminescence;Functional Materials;Highly Purified Reagents;Other Categories;Phenanthrolines;Refined Products by Sublimation;White crystalline powder;White crystalline powder;MOFS COFS
Mol File:1662-01-7.mol
Bathophenanthroline Structure
Bathophenanthroline Chemical Properties
Melting point 218-220 °C(lit.)
Boiling point 459.52°C (rough estimate)
density 1.2047 (rough estimate)
refractive index 1.7620 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in organic solvents. Slightly soluble in acidic aqueous solutions. Insoluble in neutral or alkaline solutions.
pka4.83±0.10(Predicted)
form Crystalline Powder, Crystals or Crystalline Mass
color White to yellow to pinkish
BRN 261048
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyDHDHJYNTEFLIHY-UHFFFAOYSA-N
CAS DataBase Reference1662-01-7(CAS DataBase Reference)
NIST Chemistry Reference1,10-Phenanthroline, 4,7-diphenyl-(1662-01-7)
EPA Substance Registry System1,10-Phenanthroline, 4,7-diphenyl- (1662-01-7)
Absorptionλmax?272 nm (in THF)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
RTECS SF8427000
8
TSCA Yes
HS Code 29339990
MSDS Information
ProviderLanguage
Bathophenanthroline English
ACROS English
SigmaAldrich English
ALFA English
Bathophenanthroline Usage And Synthesis
ClassificationHole-blocking layer (HBL) materials , Electron injection layer (EIL) materials, OLEDS, Organic photovoltaics, Perovskite solar cells.
ApplicationsBPhen is widely used as a hole-blocking or exciton-blocking layer due to its wide energy gap and high ionisation potential.
The phenanthroline unit is small, rigid, and planar, with extended π-electrons and short hopping lengths that facilitate electron mobility. The electron mobility of BPhen is about 5 × 10-4 cm2 V-1 s-1, which is about two orders of magnitude higher than that of Alq3.
When doped with lithium, BPhen:Li is an excellent electron-transport material, and is often used as an electron-injection layer to enable ohmic contact to any electrode -- without the need to consider the work function alignments.

Reactions
  1. Bidentate ligand and reagent for determination of iron.
  2. Ligand used in the copper-catalyzed protodecarboxylation of aromatic carboxylic acids. 
DescriptionBPhen is widely used as a hole-blocking or exciton-blocking layer due to its wide energy gap and high ionisation potential.
Chemical Propertieswhite to faintly yellow crystalline powder
UsesBathophenanthroline is widely used for determination of iron in serum and urine by colorimtetry. It acts as buffer layer to improve the efficiency of organic photovoltaic cells. It is very useful as a scavenger reagent, for the removal of traces of iron and copper from reagent solutions, which is used in the trace metal determination. Iron bathophenanthroline complex is involved as a redox mediating agent for imaging surface immobilized deoxyribonucleic acid (DNA) by using Scanning Electrochemical Microscopy (SECM).
UsesBathophenanthroline was used in an ultra-sensitive and selective nonextractive quenchofluorimetric method, in order to determine palladium (II) at μg/l Levels. It may also be used as the buffer layer to improve the performance of organic photovoltaic cells.
DefinitionChEBI: A member of the class of phenanthrolines that is 1,10-phenanthroline bearing two phenyl substituents at positions 4 and 7.
General DescriptionThis product has been enhanced for catalysis.
Bathophenanthroline Preparation Products And Raw materials
Raw materialsEthanol-->Sodium hydroxide-->Methanol-->Sulfuric acid-->PETROLEUM ETHER-->Benzene-->STANNOUS CHLORIDE-->2-Nitroaniline-->ARSENIC ACID,HEMIHYDRATE-->3-Chloropropiophenone
1,7-PHENANTHROLINE Bathocuproine Biphenyl TRIS-(BATHOPHENANTHROLINE-DISULFONATE)-RUTHENIUM(II) NA-SOLUTION Diphenylmethane 3,4'-DIAMINODIPHENYLMETHANE Bathophenanthroline: (Use 1,10-o-Phenanthroline) Bathophenanthroline Diphenylsilane TRIS(BATHOPHENANTHROLINE)NICKEL-(II) NITRATE Chlorodiphenylphosphine TRIS-(BATHOPHENANTHROLINE) RUTHENIUM (II) TETRAPHENYLBORON BATHOCUPROIN DISULPHONIC ACID DISODIUM SALT TRIS(4 7-DIPHENYL-1 10-PHENANTHROLINE) BATHOCUPROINEDISULFONIC ACID DISODIUM SALT 1,5-Diphenylcarbazide tert-Butylchlorodiphenylsilane 1,3-Diphenyl-2-thiourea

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